Xiao Mei Ouyang

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

Qing Yin Zheng, Denise Yan, Xiao Mei Ouyang et al. · Human Molecular Genetics · 2004 · 147 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population

Xiao Mei Ouyang, Denise Yan, Li Du et al. · Human Genetics · 2005 · 135 citations

Life Sciences, Genetics, Molecular Genetics +10

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Xue-Zhong Liu, Yongyi Yuan, Denise Yan et al. · Human Genetics · 2008 · 116 citations

Life Sciences, Genetics, Molecular Genetics +16

Evidence of a founder effect for the 235delC mutation of GJB2 (connexin�26) in east Asians

Denise Yan, Hong-Joon Park, Xiao Mei Ouyang et al. · Human Genetics · 2003 · 106 citations

Life Sciences, Genetics, Molecular Genetics +9

Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the <i>GJB2</i> gene and hearing loss

Denise Yan, Xiao Mei Ouyang, Simón I. Angeli et al. · American Journal of Medical Genetics Part A · 2007 · 81 citations

Life Sciences, Genetics, Molecular Genetics +12